GB986200A - Stabilization of ester group-containing synthetic resins - Google Patents
Stabilization of ester group-containing synthetic resinsInfo
- Publication number
- GB986200A GB986200A GB43077/61A GB4307761A GB986200A GB 986200 A GB986200 A GB 986200A GB 43077/61 A GB43077/61 A GB 43077/61A GB 4307761 A GB4307761 A GB 4307761A GB 986200 A GB986200 A GB 986200A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polycarbodiimide
- acid
- diisocyanate
- stearic acid
- ethylene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229920003002 synthetic resin Polymers 0.000 title abstract 5
- 239000000057 synthetic resin Substances 0.000 title abstract 5
- 125000004185 ester group Chemical group 0.000 title abstract 2
- 230000006641 stabilisation Effects 0.000 title 1
- 238000011105 stabilization Methods 0.000 title 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 9
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 abstract 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Substances OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 7
- 235000021355 Stearic acid Nutrition 0.000 abstract 5
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 5
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract 5
- 239000008117 stearic acid Substances 0.000 abstract 5
- 239000001361 adipic acid Substances 0.000 abstract 4
- 235000011037 adipic acid Nutrition 0.000 abstract 4
- 229920000728 polyester Polymers 0.000 abstract 4
- 239000004814 polyurethane Substances 0.000 abstract 4
- 229920002635 polyurethane Polymers 0.000 abstract 4
- LGXAANYJEHLUEM-UHFFFAOYSA-N 1,2,3-tri(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC(C(C)C)=C1C(C)C LGXAANYJEHLUEM-UHFFFAOYSA-N 0.000 abstract 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 3
- 239000006229 carbon black Substances 0.000 abstract 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 abstract 2
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 abstract 2
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 abstract 2
- 235000012239 silicon dioxide Nutrition 0.000 abstract 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 abstract 1
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 abstract 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 abstract 1
- WONRDHPFOHAWOG-UHFFFAOYSA-N 2-chloronaphthalen-1-ol Chemical compound C1=CC=C2C(O)=C(Cl)C=CC2=C1 WONRDHPFOHAWOG-UHFFFAOYSA-N 0.000 abstract 1
- 229940054266 2-mercaptobenzothiazole Drugs 0.000 abstract 1
- IGDCJKDZZUALAO-UHFFFAOYSA-N 2-prop-2-enoxypropane-1,3-diol Chemical compound OCC(CO)OCC=C IGDCJKDZZUALAO-UHFFFAOYSA-N 0.000 abstract 1
- BIISIZOQPWZPPS-UHFFFAOYSA-N 2-tert-butylperoxypropan-2-ylbenzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC=C1 BIISIZOQPWZPPS-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 abstract 1
- 229920002125 Sokalan® Polymers 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 abstract 1
- YGCOKJWKWLYHTG-UHFFFAOYSA-N [[4,6-bis[bis(hydroxymethyl)amino]-1,3,5-triazin-2-yl]-(hydroxymethyl)amino]methanol Chemical compound OCN(CO)C1=NC(N(CO)CO)=NC(N(CO)CO)=N1 YGCOKJWKWLYHTG-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 229920000180 alkyd Polymers 0.000 abstract 1
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 125000006267 biphenyl group Chemical group 0.000 abstract 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 abstract 1
- GWOWVOYJLHSRJJ-UHFFFAOYSA-L cadmium stearate Chemical compound [Cd+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O GWOWVOYJLHSRJJ-UHFFFAOYSA-L 0.000 abstract 1
- VPKDCDLSJZCGKE-UHFFFAOYSA-N carbodiimide group Chemical group N=C=N VPKDCDLSJZCGKE-UHFFFAOYSA-N 0.000 abstract 1
- 150000001718 carbodiimides Chemical class 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 239000006232 furnace black Substances 0.000 abstract 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 abstract 1
- 239000012948 isocyanate Substances 0.000 abstract 1
- 150000002513 isocyanates Chemical class 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- 150000004702 methyl esters Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 1
- 239000004584 polyacrylic acid Substances 0.000 abstract 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 abstract 1
- -1 polyesterurethanes Substances 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 229920002689 polyvinyl acetate Polymers 0.000 abstract 1
- 239000011118 polyvinyl acetate Substances 0.000 abstract 1
- 230000001698 pyrogenic effect Effects 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 230000000087 stabilizing effect Effects 0.000 abstract 1
- 235000011150 stannous chloride Nutrition 0.000 abstract 1
- 239000001119 stannous chloride Substances 0.000 abstract 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 229920006305 unsaturated polyester Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B5/00—Preserving by using additives, e.g. anti-oxidants
- C11B5/0042—Preserving by using additives, e.g. anti-oxidants containing nitrogen
- C11B5/0057—Amides or imides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
- C08L101/02—Compositions of unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C08L101/06—Compositions of unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing oxygen atoms
- C08L101/08—Carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/06—Unsaturated polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
- C08L75/06—Polyurethanes from polyesters
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/907—Polycarbodiimide
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Polyurethanes Or Polyureas (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Abstract
A process for stabilizing ester group-containing synthetic resins comprises incorporating in the synthetic resin at any convenient stage in its production or in the finished resin, a polycarbodiimide having a molecular weight of at least about 500 and having more than 3 carbodiimide groups. Specified synthetic resins are those derived by reacting a polyfunctional carboxylic acid with a polyfunctional alcohol, if desired with the concurrent use of a monofunctional acid or alcohol, polyesteramides, polyesterurethanes, synthetic resins derived from naturally occurring esters, polyesters containing styrene residues and unsaturated polyesters, many suitable reactants for making the polymers being listed. Specified carbodiimides are those derived from isocyanates. The examples disclose compositions comprising:-(1) a polyester polyurethane made from ethylene and propylene glycol, adipic acid, 4-41-diphenyl methane diisocyanate and butane diol, carbon black, stearic acid, t-butyl cumyl peroxide, triallyl cyanurate and triisopropyl benzene polycarbodiimides; (2) a maleic anhydride/propylene glycol alkyd and a polycarbodiimide made from 2:4:6-triethylphenylene-1:3-diisocyanate; (3) an ethylene/vinyl acetate copolymer, stearic acid, silicic acid, dicumyl peroxide and 1:3:5-triisopropylbenzene polycarbodiimide; (4) a polyurethane made from adipic acid, ethylene glycol, monoethanolamine and hexamethylene diisocyanate, furnace black, hexamethylol melamine, chloronaphthol and triisopropyl benzene polycarbodiimide; (5) a polyester polyurethane made from adipic acid, ethylene and propylene glycol, 4:41-diphenyl methane diisocyanate and glycerol monoallyl ether, stearic acid, pyrogenic silicic acid, cadmium stearate, sulphur, 2-mercapto benzothiazole, an addition product of mercaptobenzothiazyl disulphide and stannous chloride and triisopropyl benzene polycarbodiimide; (6) a polyester polyurethane made from diethylene and butylene glycol, adipic acid and 2:4- and 2:6-toluylene diisocyanate, stearic acid, carbon black, dimerized 2:4-toluylene diisocyanate and 1:3:5-triisopropyl benzene polycarbodiimide; (7) polyacrylic acid methyl ester, stearic acid, carbon black, dicumyl peroxide, triallylcyanurate and 1-methyl-3:5-diethyl benzene polycarbodiimide and (8) polyvinyl acetate and a polycarbodiimide made from 3:5:31:51-tetraisopropyl diphenyl methane-4:4-diisocyanate. Specifications 851,936 and 930,036 are referred to.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF32679A DE1285747B (en) | 1960-12-02 | 1960-12-02 | Carbodiimides as plastic stabilizers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB986200A true GB986200A (en) | 1965-03-17 |
Family
ID=7094733
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB43077/61A Expired GB986200A (en) | 1960-12-02 | 1961-12-01 | Stabilization of ester group-containing synthetic resins |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3193522A (en) |
| BE (1) | BE610969A (en) |
| CH (1) | CH409392A (en) |
| DE (1) | DE1285747B (en) |
| FR (1) | FR1310138A (en) |
| GB (1) | GB986200A (en) |
| NL (1) | NL272088A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0803538A3 (en) * | 1996-04-26 | 1998-04-15 | Nisshinbo Industries, Inc. | Hydrolysis stabilizer for ester group-containing resin and process for hydrolysis stabilization of ester group-containing resin using said hydrolysis stabilizer |
| US6498225B2 (en) * | 2000-03-29 | 2002-12-24 | Rhein Chemie Rheinau Gmbh | Polycarbodiimide-based block copolymers, a method of preparing them and their use as hydrolysis stabilizers |
| WO2013030147A2 (en) | 2011-08-29 | 2013-03-07 | Bayer Intellectual Property Gmbh | A process for preparing plastics with improved hydrolysis stability, the plastics prepared from the same and uses thereof |
| US20150090318A1 (en) * | 2011-08-22 | 2015-04-02 | Rhein Chemie Rheinau Gmbh | Novel film for solar cells |
Families Citing this family (65)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1223101B (en) * | 1963-10-25 | 1966-08-18 | Bayer Ag | Polyaether urethane threads stabilized against light and heat |
| DE1243811B (en) * | 1964-06-16 | 1967-07-06 | Bayer Ag | Lubricant additives |
| GB1224635A (en) * | 1967-04-03 | 1971-03-10 | Fiber Industries Inc | Stabilised polyester shaped articles |
| NL136653C (en) * | 1970-01-24 | |||
| US3716502A (en) * | 1970-11-27 | 1973-02-13 | Inmont Corp | Elastomeric thermoplastic polyester polyurethane compositions stabilized against hydrolysis |
| CA994036A (en) * | 1971-03-02 | 1976-07-27 | William K. Witsiepe | Stabilized elastomeric copolyetherester compositions |
| US3852101A (en) * | 1972-11-01 | 1974-12-03 | Monsanto Co | Stabilization of polyester fibers with carbodiimide |
| US3975329A (en) * | 1974-01-02 | 1976-08-17 | The Goodyear Tire & Rubber Company | Industrial polyester yarn |
| US4048128A (en) * | 1974-02-20 | 1977-09-13 | E. I. Du Pont De Nemours And Company | Thermally stabilized segmented copolyester adhesive |
| US3915935A (en) * | 1974-02-28 | 1975-10-28 | Usm Corp | Polyurethane adhesive comprising a polyester and a prepolymer of the same polyester |
| CA1056985A (en) * | 1975-03-17 | 1979-06-19 | Celanese Corporation | Polyesters for extrusion applications |
| CA1088235A (en) * | 1975-09-24 | 1980-10-21 | Frank M.. Berardinelli | Reinforced polyester composition having improved impact strength |
| US4052360A (en) * | 1975-09-24 | 1977-10-04 | Celanese Corporation | Reinforced flame retardant polyester composition having non-drip characteristics |
| US4066629A (en) * | 1976-10-28 | 1978-01-03 | Celanese Corporation | Process for preparing carbodiimides utilizing a phosphonium salt catalyst |
| JPS53107794A (en) * | 1977-03-03 | 1978-09-20 | Kao Corp | Abraisives |
| DE2724411C2 (en) * | 1977-05-28 | 1982-12-02 | Dynamit Nobel Ag, 5210 Troisdorf | Process for the production of polytetramethylene terephthalate |
| US4113676A (en) * | 1977-05-31 | 1978-09-12 | Ppg Industries, Inc. | Aqueous dispersions of esters stabilized with carbodiimides |
| US4306052A (en) * | 1980-09-25 | 1981-12-15 | The Upjohn Company | Thermoplastic polyester polyurethanes |
| DE3269641D1 (en) * | 1981-09-09 | 1986-04-10 | Ciba Geigy Ag | Stabilised thermoplastic polyester compositions |
| US4977219A (en) * | 1983-02-24 | 1990-12-11 | Union Carbide Chemicals And Plastics Company, Inc. | Low temperature crosslinking of water-borne resins |
| US4487964A (en) * | 1983-02-24 | 1984-12-11 | Union Carbide Corporation | Method of making mixed aliphatic/aromatic polycarbodiimides |
| US4845161A (en) * | 1983-02-25 | 1989-07-04 | E. I. Du Pont De Nemours And Company | Polyoxymethylene/polyurethane compositions containing polycarbodiimide |
| CA1246768A (en) * | 1983-02-25 | 1988-12-13 | Paul N. Richardson | Polyoxymethylene/polyurethane compositions containing polycarbodiimide |
| US4452965A (en) * | 1983-07-29 | 1984-06-05 | The Goodyear Tire & Rubber Company | Random elastomeric copolyesters |
| DE3331436A1 (en) * | 1983-08-31 | 1985-03-21 | Bayer Ag, 5090 Leverkusen | BISMORPHOLINE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A HYDROLYSIS PROTECT |
| JPS60210659A (en) * | 1984-04-04 | 1985-10-23 | Polyplastics Co | Polyester composition with excellent hot water resistance |
| US4859741A (en) * | 1984-04-04 | 1989-08-22 | Polyplastics Co., Ltd. | Polyester composition |
| US4542177A (en) * | 1984-06-29 | 1985-09-17 | Mobay Chemical Corporation | Thermoplastic polyester molding composition having an improved impact performance |
| US4772649A (en) * | 1986-12-18 | 1988-09-20 | The Dow Chemical Company | Polyesteramide and sufficient carbodiimide to impart improved compression set |
| EP0282072B1 (en) * | 1987-03-13 | 1994-06-22 | Kuraray Co., Ltd. | Stabilized poly(beta-methyl-delta-valerolactone) |
| US4861828A (en) * | 1987-04-06 | 1989-08-29 | E. I. Du Pont De Nemours And Company | Toughened thermoplastic polyarylate-polyamide compositions |
| US4952621A (en) * | 1988-06-06 | 1990-08-28 | The B. F. Goodrich Company | Urethane sealants or coating admixtures having improved shelf stability |
| DE3930845A1 (en) * | 1989-09-15 | 1991-03-28 | Hoechst Ag | POLYESTER FIBERS MODIFIED WITH CARBODIIMIDES AND METHOD FOR THEIR PRODUCTION |
| US5248713A (en) * | 1990-06-13 | 1993-09-28 | Raychem Corporation | Stabilized polymeric compositions |
| JP3228977B2 (en) * | 1991-03-14 | 2001-11-12 | ジョーンズ・マンヴィル・インターナショナル・インコーポレーテッド | Carbodiimide-modified polyester fiber and method for producing the same |
| WO1994022956A1 (en) * | 1993-04-05 | 1994-10-13 | Alliedsignal Inc. | High impact polyester compositions |
| US5597942A (en) * | 1993-06-08 | 1997-01-28 | Basf Aktiengesellschaft | Carbodiimides and/or oligomeric polycarbodiimides based on 1 3-bis (1-methyl-1-isocyanatoethyl) benzene their use as hydrolysis stabilizers |
| US5504241A (en) * | 1994-05-12 | 1996-04-02 | Basf Aktiengesellschaft | Carbodiimides and/or oligomeric polycarbodiimides based on 1,3-bis(1-methyl-1-isocyanatoethyl)benzene, their preparation, and their use as hydrolysis stabilizers |
| DE4435548A1 (en) * | 1994-10-05 | 1996-04-11 | Rhein Chemie Rheinau Gmbh | Stabilized lubricant base substance |
| US5886088A (en) * | 1995-02-23 | 1999-03-23 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Polyethylene terephthalate resin composition |
| JP3422642B2 (en) * | 1996-12-24 | 2003-06-30 | 日清紡績株式会社 | Agent and method for improving resistance of ester-containing resin to degradation by microorganisms |
| US6147128A (en) * | 1998-05-14 | 2000-11-14 | Astenjohnson, Inc. | Industrial fabric and yarn made from recycled polyester |
| DE19842152A1 (en) | 1998-09-15 | 2000-03-16 | Bayer Ag | High viscosity polyester preparation for molding involves using low and high viscosity polyesters |
| US6143702A (en) * | 1998-10-09 | 2000-11-07 | Exxon Research And Engineering Company | Lubricating oils of enhanced oxidation stability containing n-phenyl-naphthyl amines, or substituted derivatives of n-phenyl naphthyl amine and carbodiimide acid scavengers |
| DE50004222D1 (en) | 1999-07-02 | 2003-12-04 | Rhein Chemie Rheinau Gmbh | Catalyst system for the NCO / OH reaction (polyurethane formation) |
| US7008983B2 (en) * | 2002-04-29 | 2006-03-07 | E. I. Du Pont De Nemours And Company | Hydrolysis resistant polyester compositions and related articles and methods |
| US20030216500A1 (en) * | 2002-04-29 | 2003-11-20 | Mckenna James Michael | Hydrolysis resistant polyester elastomer compositions and related articles and methods |
| US6818293B1 (en) * | 2003-04-24 | 2004-11-16 | Eastman Chemical Company | Stabilized polyester fibers and films |
| DE10326380A1 (en) | 2003-06-12 | 2004-12-30 | Rhein-Chemie Rheingau Gmbh | Compatible blends of thermoplastic molding compounds |
| US7119141B2 (en) | 2003-08-20 | 2006-10-10 | General Electric Company | Polyester molding composition |
| ES2337487T3 (en) * | 2005-09-21 | 2010-04-26 | Raschig Gmbh | FORMULATIONS THAT INCLUDE STABILIZING AGENTS AGAINST HYDROLYSIS. |
| JP5546241B2 (en) * | 2006-05-31 | 2014-07-09 | ザ シャーウィン−ウィリアムズ カンパニー | Dispersion polymer |
| DE102007056631A1 (en) * | 2007-11-24 | 2009-05-28 | Teijin Monofilament Germany Gmbh | Resistant to hydrolysis, process for their preparation and their use |
| US8829112B1 (en) | 2008-01-09 | 2014-09-09 | E I Du Pont De Nemours And Company | Polyester composition resistant to hydrolysis |
| KR20100112610A (en) * | 2008-01-09 | 2010-10-19 | 이 아이 듀폰 디 네모아 앤드 캄파니 | Polyester composition resistant to hydrolysis |
| JP5325426B2 (en) * | 2008-02-06 | 2013-10-23 | オリンパスメディカルシステムズ株式会社 | Elastomer molded body for endoscope |
| JP5405862B2 (en) * | 2008-03-31 | 2014-02-05 | ウィンテックポリマー株式会社 | Multilayer tube |
| EP2520597A1 (en) * | 2011-05-05 | 2012-11-07 | Rhein Chemie Rheinau GmbH | Carbodiimides made of trisubstituted aromatic isocyanates, method for their manufacture and application thereof |
| US9199925B2 (en) | 2011-05-05 | 2015-12-01 | Rhein Chemie Rheinau Gmbh | Carbodiimides from trisubstituted aromatic isocyanates, a method for producing same, and the use of same |
| CA2863100C (en) | 2012-02-17 | 2020-07-07 | Andersen Corporation | Polylactic acid containing building component |
| KR102049410B1 (en) | 2013-06-11 | 2019-11-27 | 에스케이케미칼 주식회사 | Parts for vehicle, electrical/electronic instrument, home appliance, office machine, or household item |
| EP2933285B1 (en) | 2014-04-15 | 2019-01-09 | Raschig GmbH | Hydrolysis stabiliser formulations |
| WO2016007119A1 (en) | 2014-07-07 | 2016-01-14 | Halliburton Energy Services, Inc. | Downhole tools comprising aqueous-degradable sealing elements |
| NO348480B1 (en) * | 2014-07-07 | 2025-02-03 | Halliburton Energy Services Inc | Downhole Tools Comprising Aqueous-Degradable Elastomer Sealing Elements With Carbodiimide |
| EP3945110A1 (en) | 2020-07-30 | 2022-02-02 | Clariant International Ltd | Flame retardant stabilizer combinations for flame-resistant polymers having improved resistance to hydrolysis and their use |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2941983A (en) * | 1957-05-07 | 1960-06-21 | Du Pont | Urethane-terminated polycarbodiimides |
-
0
- FR FR1310138D patent/FR1310138A/fr not_active Expired
- NL NL272088D patent/NL272088A/xx unknown
-
1960
- 1960-12-02 DE DEF32679A patent/DE1285747B/en not_active Ceased
-
1961
- 1961-11-23 CH CH1364561A patent/CH409392A/en unknown
- 1961-11-29 US US155791A patent/US3193522A/en not_active Expired - Lifetime
- 1961-11-30 BE BE610969A patent/BE610969A/en unknown
- 1961-12-01 GB GB43077/61A patent/GB986200A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0803538A3 (en) * | 1996-04-26 | 1998-04-15 | Nisshinbo Industries, Inc. | Hydrolysis stabilizer for ester group-containing resin and process for hydrolysis stabilization of ester group-containing resin using said hydrolysis stabilizer |
| US6498225B2 (en) * | 2000-03-29 | 2002-12-24 | Rhein Chemie Rheinau Gmbh | Polycarbodiimide-based block copolymers, a method of preparing them and their use as hydrolysis stabilizers |
| US20150090318A1 (en) * | 2011-08-22 | 2015-04-02 | Rhein Chemie Rheinau Gmbh | Novel film for solar cells |
| WO2013030147A2 (en) | 2011-08-29 | 2013-03-07 | Bayer Intellectual Property Gmbh | A process for preparing plastics with improved hydrolysis stability, the plastics prepared from the same and uses thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| US3193522A (en) | 1965-07-06 |
| FR1310138A (en) | 1963-03-06 |
| DE1285747B (en) | 1968-12-19 |
| NL272088A (en) | |
| BE610969A (en) | 1962-03-16 |
| CH409392A (en) | 1966-03-15 |
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